Peroxisomal Import of Human Alanine:glyoxylate Aminotransferase Requires Ancillary Targeting Information Remote from Its C Terminus-Reference-Cited by-同舟云学术

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Peroxisomal Import of Human Alanine:glyoxylate Aminotransferase Requires Ancillary Targeting Information Remote from Its C Terminus

Published:2005-07 Issue:29 Volume:280 Page:27111-27120
ISSN:0021-9258
Container-title:Journal of Biological Chemistry
language:en
Short-container-title:Journal of Biological Chemistry

Author:

Huber Pia A.J.,Birdsey Graeme M.,Lumb Michael J.,Prowse David T.R.,Perkins Tommy J.,Knight Daniel R.,Danpure Christopher J.

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference44 articles.

1. The Metabolic and Molecular Bases of Inherited Disease;Danpure,2001

2. An enzyme trafficking defect in two patients with primary hyperoxaluria type 1: peroxisomal alanine/glyoxylate aminotransferase rerouted to mitochondria.

3. Identification of mutations associated with peroxisome-to-mitochondrion mistargeting of alanine/glyoxylate aminotransferase in primary hyperoxaluria type 1.

4. Mistargeting of peroxisomal L-alanine:glyoxylate aminotransferase to mitochondria in primary hyperoxaluria patients depends upon activation of a cryptic mitochondrial targeting sequence by a point mutation.

5. Inhibition of alanine:glyoxylate aminotransferase 1 dimerization is a prerequisite for its peroxisome-to-mitochondrion mistargeting in primary hyperoxaluria type 1.

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1. Biochemical and cellular effects of a novel missense mutation of the AGXT gene associated with Primary Hyperoxaluria Type 1;Biochemical and Biophysical Research Communications;2023-02

2. Studying the interaction between PEX5 and its full-length cargo proteins in living cells by a novel Försteŕs resonance energy transfer-based competition assay;Frontiers in Cell and Developmental Biology;2022-11-03

3. Pls1 Is a Peroxisomal Matrix Protein with a Role in Regulating Lysine Biosynthesis;Cells;2022-04-22

4. A Putative Mutation Hotspot of the AGXT Gene Associated with Primary Hyperoxaluria Type 1 in the Chinese Population;The Tohoku Journal of Experimental Medicine;2018

5. Folding Defects Leading to Primary Hyperoxaluria;Targeting Trafficking in Drug Development;2017

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